37D2-37D5;38A6-38B2
37D2-37D7;38A6-38B2
37C6-37D1;38A6-38B2
γTub37C << bk1 << l(2)37Dd << l(2)37Fg << bk2 << pr
Copy number variation (CNV) analysis identifies a deletion on chromosome 2L with breakpoints occurring in approximately 3kb windows whose midpoints are coordinates 2L:19423344 and 2L:19962150 .
Viable and female fertile in combination with Df(2L)be408. Viable and fertile in combination with Df(2L)pr2b. Viable and fertile in combination with Df(2L)pr37. Viable, male fertile and female subfertile in combination with Df(2L)pr11163. Viable and fertile in combination with Df(2L)pr-M1. Lethal in combination with Df(2L)pr49. Lethal in combination with Df(2L)pr8311. Lethal in combination with Df(2L)pr1122. Lethal in combination with Df(2L)TW1. Lethal in combination with Df(2L)TW161.
The Df(2L)Sd37 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).
Ref: FBrf0030142.
Left limit of break 1 from polytene analysis (FBrf0030142) Right limit of break 1 from inclusion of RanGap (FBrf0030142) Limits of break 2 from polytene analysis (FBrf0030142)